Canonical Allele Identifier: CA1793761

Gene: CNGA3

Linked Data

• dbSNP Id: rs759796739
• ExAC: 2:99006125 A / G
• gnomAD v2: 2-99006125-A-G
• gnomAD v4: 2-98389662-A-G
• MyVariant Identifiers: chr2:g.99006125A>G (hg19) ; chr2:g.98389662A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389662A>G , CM000664.2:g.98389662A>G	GRCh38
NC_000002.11:g.99006125A>G , CM000664.1:g.99006125A>G	GRCh37
NC_000002.10:g.98372557A>G	NCBI36
NG_009097.1:g.48508A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.454A>G MANE Select	ENSP00000272602.2:p.Lys152Glu
ENST00000272602.6:c.454A>G	ENSP00000272602.2:p.Lys152Glu
ENST00000393503.2:n.459A>G
ENST00000393504.5:c.454A>G	ENSP00000377140.1:p.Lys152Glu
ENST00000409937.1:c.466A>G	ENSP00000386761.1:p.Lys156Glu
ENST00000436404.6:c.400A>G	ENSP00000410070.2:p.Lys134Glu
NM_001079878.1:c.400A>G	NP_001073347.1:p.Lys134Glu
NM_001298.2:c.454A>G	NP_001289.1:p.Lys152Glu
XM_006712243.2:c.565A>G	XP_006712306.1:p.Lys189Glu
XM_011510554.1:c.619A>G	XP_011508856.1:p.Lys207Glu
XM_011510554.2:c.619A>G	XP_011508856.1:p.Lys207Glu
NM_001079878.2:c.400A>G	NP_001073347.1:p.Lys134Glu
NM_001298.3:c.454A>G MANE Select	NP_001289.1:p.Lys152Glu